Sr. Manager, Quality Engineering

Who We Are

ABOUT ENOVIS

Enovis Corporation (NYSE : ENOV) is an innovation-driven medical technology growth company dedicated to developing clinically differentiated solutions that generate measurably better patient outcomes and transform workflows. Powered by a culture of continuous improvement, global talent and innovation, the Company's extensive range of products, services and integrated technologies fuels active lifestyles in orthopedics and beyond. For more information about Enovis, please visit www.enovis.com .

What You'll Do

At Enovis we sweat the little things. We embrace collaboration with our partners and patients, and we glory in the grind of scientific excellence - with the goal of transforming medical technology as we know it.

Because that's how we change the lives of patients for the better. And that's how we create better together.

As a key member of the Quality Assurance team, you will play an integral part in helping Enovis drive the medical technology industry forward through transforming patient care and creating better patient outcomes.

Job Title :

Sr. Manager, Quality Engineering

Reports To :

Sr Director, Quality Assurance

Location : Austin, TX

Business Unit Description :

Recon, Quality

High Level Position Summary :

The Quality Engineering Sr. Manager is responsible for leading a team of quality engineers in driving product and process excellence across the surgical device portfolio. This role ensures compliance with regulatory standards, support manufacturing as well as new product introduction and fosters a culture of continuous improvement. The Quality Engineering Sr. Manager will collaborate cross-functionally to implement quality strategies that enhance product reliability, reduce risk, and improve operational efficiency.

Key Responsibilities :

• Lead and mentor a team of quality engineers, providing technical guidance and performance management.
• Develop and implement quality strategies that align with business objectives and regulatory requirements.
• Lead quality engineering support for manufacturing operations, ensuring robust process controls, effective risk management, and validation of production methods.
• Ensure compliance with FDA QSR (21 CFR Part 820), ISO 13485, and ISO 14971 standards.
• Drive root cause analysis and corrective / preventive actions (CAPA) for product and process issues.
• Collaborate with Manufacturing, R&D, Regulatory Affairs, and Supply Chain to resolve quality challenges and improve processes.
• Support internal and external audits, acting as a subject matter expert for quality engineering practices.
• Maintain and improve quality system documentation, including procedures, work instructions, and validation protocols.

Minimum Qualifications

Preferred Qualifications

"Creating better together". It's the Enovis purpose, and it's what drives us and empowers us every day on a global scale. We know that the power to create better - for our customers, our team members, and our shareholders - begins with having the best team, pursuing common goals, operating at the highest levels, and delivering extraordinary outcomes.

EOE AA M / F / VET / Disability Statement

All qualified applicants will receive consideration for employment and will not be discriminated against on the basis of race, religion, color, national origin, sex, protected veteran status, disability, or any other basis protected by federal, state or local laws.